ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System
K-Number: K173981 · 2018-02-02
Device Summary
Frequently Asked Questions
What is the ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System?
ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2018-02-02. It is manufactured by Siemens Medical Solutions USA, Inc. Ultrasound Group. The 510(k) number is K173981.
When was ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System approved by the FDA?
ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System received FDA 510(k) clearance on 2018-02-02, under approval number K173981.
What company makes ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System?
ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System is manufactured by Siemens Medical Solutions USA, Inc. Ultrasound Group.
What is the FDA product code for ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System?
The FDA product code for ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System is IYN.
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Related PubMed Literature
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.